Canonical Allele Identifier: CA359563385

Gene: RICTOR

Linked Data

• MyVariant Identifiers: chr5:g.38955710G>C (hg19) ; chr5:g.38955608G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.38955608G>C , CM000667.2:g.38955608G>C	GRCh38
NC_000005.9:g.38955710G>C , CM000667.1:g.38955710G>C	GRCh37
NC_000005.8:g.38991467G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296782.10:c.2596C>G	ENSP00000296782.5:p.Arg866Gly
ENST00000503698.2:c.556C>G	ENSP00000518563.1:p.Arg186Gly
ENST00000514735.2:c.2548C>G	ENSP00000423162.2:p.Arg850Gly
ENST00000711063.1:c.2596C>G	ENSP00000518562.1:p.Arg866Gly
ENST00000357387.8:c.2596C>G MANE Select	ENSP00000349959.3:p.Arg866Gly
ENST00000296782.9:c.2596C>G	ENSP00000296782.5:p.Arg866Gly
ENST00000357387.7:c.2596C>G	ENSP00000349959.3:p.Arg866Gly
ENST00000503698.1:n.556C>G
ENST00000511516.5:c.*1820C>G	ENSP00000423019.1:n.*1820C>G
NM_001285439.1:c.2596C>G	NP_001272368.1:p.Arg866Gly
NM_001285440.1:c.1741C>G	NP_001272369.1:p.Arg581Gly
NM_152756.4:c.2596C>G	NP_689969.2:p.Arg866Gly
XM_006714463.2:c.2596C>G	XP_006714526.1:p.Arg866Gly
XM_011514005.1:c.2596C>G	XP_011512307.1:p.Arg866Gly
XM_011514006.1:c.2407C>G	XP_011512308.1:p.Arg803Gly
XM_011514007.1:c.1741C>G	XP_011512309.1:p.Arg581Gly
XM_006714463.3:c.2596C>G	XP_006714526.1:p.Arg866Gly
XM_011514005.2:c.2596C>G	XP_011512307.1:p.Arg866Gly
XM_011514006.3:c.2407C>G	XP_011512308.1:p.Arg803Gly
XM_017009311.1:c.2548C>G	XP_016864800.1:p.Arg850Gly
XM_017009312.1:c.2548C>G	XP_016864801.1:p.Arg850Gly
XM_017009313.1:c.2437C>G	XP_016864802.1:p.Arg813Gly
XM_017009314.2:c.1741C>G	XP_016864803.1:p.Arg581Gly
XM_017009315.2:c.1741C>G	XP_016864804.1:p.Arg581Gly
NM_152756.5:c.2596C>G MANE Select	NP_689969.2:p.Arg866Gly
NM_001285439.2:c.2596C>G	NP_001272368.1:p.Arg866Gly
NM_001285440.2:c.1741C>G	NP_001272369.1:p.Arg581Gly